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Chemical Synthesis with out using solvents has constructed right into a strong method because it reduces the volume of poisonous waste produced and accordingly turns into much less destructive to the surroundings. Koichi Tanaka discusses the most recent advancements during this box, giving emphasis at the expertise used in addition to the sensible functions.
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Angew. , Int. Ed. 1997, 36, 673–685. 4. Lopez, R. ; Hays, D. ; Fu, G. C. J. Am. Chem. Soc. 1997, 119, 6949–6950. 5. Hansen, H. ; Kehler, J. Synthesis 1999, 1925–1930. 6. ; Pereyre, M. Tetrahedron Lett. 2000, 41, 3377–3380. 7. ; Roberts, B. P. Tetrahedron Lett. 2001, 42, 763–766. 8. Clive, D. L. ; Wang, J. J. Org. Chem. 2002, 67, 1192–1198. 9. Rhee, J. ; Bliss, B. ; RajanBabu, T. V. J. Am. Chem. Soc. 2003, 125, 1492–1493. 10. Gómez, A. ; López, J. C. Eur. J. Org. Chem. 2004, 1830– 1840. 11. ; Zhai, H.
S) 1984, 395. 6. ; Seno, M. J. Org. Chem. 1987, 52, 4702– 4709. 7. ; Yamamoto, S. Chem. Pharm. Bull. 1987, 35, 4465–4472. 8. ; Yoshizaki, S. Chem. Pharm. Bull. 1989, 37, 1216–1220. 9. Poyarkov, A. ; Frasinyuk, M. ; Kibirev, V. ; Poyarkova, S. A. Russ. J. Bioorg. Chem. 2006, 32, 277–279. 10. ; Crouch, G. ; Jones, J. P. Bioorg. Med. Chem. Lett. 2008, 16, 4064–4074. 1. 10 Arndt–Eistert homologation One-carbon homologation of carboxylic acids using diazomethane. O R O SOCl2 OH O 1. CH2N2 R Cl 2.
Tetrahedron Lett. 1989, 30, 2129−2132. 4. ; Petrini, M. J. Chem. , Perkin Trans. 2 1991, 657−663. Mechanistic studies. 5. ; Marcantoni, E. J. Chem. , Perkin Trans. 1 1991, 2757−2761. 6. Dobbs, A. J. Org. Chem. 2001, 66, 638−641. 7. Garg, N. ; Stoltz, B. M. J. Am. Chem. Soc. 2002, 124, 13179−13184. 8. ; Cook, J. M. Bartoli indole synthesis. In Name Reactions in Heterocyclic Chemistry; Li, J. , Corey, E. J. ; Wiley & Sons: Hoboken, NJ, 2005, pp 100−103. (Review). 9. ; Bartoli, G. Current Org. Chem.